Whether Circulating miRNAs or miRNA-Carriers Serve as Biomarkers for Acute Myocardial Infarction.

Journal of biomarkers in drug development Pub Date : 2012-08-02 eCollection Date: 2013-01-01 DOI:10.4172/jbdd.1000e103
Hongyan Zhu, Guo-Chang Fan
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引用次数: 8

Abstract

Acute myocardial infarction (AMI) remains a major cause of death in the US. An early and reliable diagnosis may warrant immediate initiation of reperfusion therapy to potentially improve the survival rate among the AMI patients. Currently, cardiac troponins (i.e. cTnT and cTnI) and creatine kinase MB (CK-MB) are widely used for AMI diagnosis. However, elevation of these biomarkers is also observed in human patients with myocarditis, aortic dissection, pulmonary embolism, congestive heart failure and renal failure. Furthermore, measurable amounts of troponin proteins are usually not released from damaged myocardium before 4 to 8 h after onset of symptoms, making an early biomarker-based diagnosis of AMI rather difficult. Therefore, new biomarkers with high sensitivity and specificity in early diagnosis of AMI are greatly needed.

循环mirna或mirna载体是否可作为急性心肌梗死的生物标志物
在美国,急性心肌梗死(AMI)仍然是导致死亡的主要原因。早期和可靠的诊断可能需要立即开始再灌注治疗,以潜在地提高AMI患者的生存率。目前,心肌肌钙蛋白(即cTnT和cTnI)和肌酸激酶MB (CK-MB)被广泛用于AMI的诊断。然而,在人类心肌炎、主动脉夹层、肺栓塞、充血性心力衰竭和肾衰竭患者中也观察到这些生物标志物的升高。此外,在症状出现后4 - 8小时,受损心肌通常不会释放出可测量量的肌钙蛋白,这使得基于生物标志物的AMI早期诊断相当困难。因此,迫切需要新的具有高灵敏度和特异性的AMI早期诊断生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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